HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894584Generated: October 28, 2026
2,6-Dimethylaniline → HCID 20512402, compound
https://huagongshe.com/reaction/894584
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dimethylaniline | HCID 6896 | — |
| Reactant | HCID 20512395 | HCID 20512395 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 20512402 | HCID 20512402 | 75.3% |
Reaction Steps
A mixture of 106.8 g (0.441 moles) of N-(β-bromopropyl)-2,6-dimethyl-aniline, obtained as described in point (a) above, 110 ml (107.4 g, 0.88 moles) of 2,6-dimethylaniline and 1.6 g (10 mmoles) of potassium iodide is stirred at 100° to 105° C. for 3 hours under nitrogen atmosphere. The mixture is allowed to cool, 600 ml of 10% aqueous hydrochloric acid are added, and the resulting mixture is allowed to stand at room temperature overnight. The separated precipitate, which is a mixture of the hydrochloride and the hydrobromide of the expected product, is filtered off, washed with water, dried, and then treated as described in point (b) of Method (b) above in order to liberate the base. In this way 93.8 g (75.3%) of 1,2-bis(2',6'-dimethylphenyl-amino)-propane are obtained; m.p.: 54°-56° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04284642 |
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| Source dataset | uspto-grants-1981_08 |
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| ORD ID | ord-9ba83dfb20d0468fb146f6c62cb68d12 |
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| Source note | uspto-grants-1981_08 |
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